ID: 130056095 | ATAC-STARR-seq lymphoblastoid active region 8728 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74493768..74493847) | | |
ID: 130056094 | ATAC-STARR-seq lymphoblastoid silent region 5931 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74493288..74493567) | | |
ID: 130056093 | ATAC-STARR-seq lymphoblastoid silent region 5930 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74493058..74493117) | | |
ID: 127827976 | H3K4me1 hESC enhancer GRCh37_chr14:74876293-74876840 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74409590..74410137) | | |
ID: 127827975 | H3K4me1 hESC enhancer GRCh37_chr14:74873841-74874342 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74407138..74407639) | | |
ID: 127827974 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74868255-74869164 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74401552..74402461) | | |
ID: 127827973 | H3K4me1 hESC enhancer GRCh37_chr14:74861891-74862391 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74395188..74395688) | | |
ID: 127827972 | H3K4me1 hESC enhancer GRCh37_chr14:74825115-74825693 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74358412..74358990) | | |
ID: 127827971 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74816188-74816937 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74349485..74350234) | | |
ID: 127827970 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74815437-74816187 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74348734..74349484) | | |
ID: 127827969 | H3K27ac hESC enhancer GRCh37_chr14:74796151-74796770 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74329448..74330067) | | |
ID: 127827968 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74794289-74794910 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74327586..74328207) | | |
ID: 127827967 | OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:74792429-74793048 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74325726..74326345) | | |
ID: 126861999 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:74954493-74955692 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74487790..74488989) | | |
ID: 100616211 | microRNA 4709 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74480133..74480204, complement) | mir-4709 | |
ID: 100287680 | SUB1 pseudogene 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74305423..74306063) | | |
ID: 646658 | synapse differentiation inducing 1 like [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74405899..74480143, complement) | CAPUCIN, DSPC1, IFITMD4, SynDIG2, TMEM90A | 609999 |
ID: 326325 | ribosomal protein S2 pseudogene 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74377687..74378623, complement) | RPS2_17_1389 | |
ID: 122961 | iron-sulfur cluster assembly 2 [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74493765..74497106) | HBLD1, ISA2, MMDS4, c14_5557 | 615317 |
ID: 55237 | vertebrae development associated [Homo sapiens (human)] | Chromosome 14, NC_000014.9 (74302993..74360008) | C14orf115, vertnin | 620468 |